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茄尼醇通过下调鞘内 T 细胞受限内抗原-1 改善完全弗氏佐剂诱导的小鼠焦虑样行为。

Solanesol Ameliorates Anxiety-like Behaviors via the Downregulation of Cingulate T Cell-Restricted Intracellular Antigen-1 in a Complete Freund's Adjuvant-Induced Mouse Model.

机构信息

School of Pharmacy, Hangzhou Normal University, Hangzhou 311121, China.

School of Basic Medical Sciences, Hangzhou Normal University, Hangzhou 311121, China.

出版信息

Int J Mol Sci. 2024 Sep 21;25(18):10165. doi: 10.3390/ijms251810165.

Abstract

Anxiety disorder is a universal disease related to neuro-inflammation. Solanesol has shown positive effects because of its anti-inflammatory, anti-tumor, and anti-ulcer properties. This study focused on determining whether solanesol could ameliorate anxiety-like behaviors in a mouse model of neuro-inflammation and identify its working targets. Complete Freund's adjuvant (CFA)-induced mice that were intra-peritoneally administered with solanesol (50 mg/kg) for 1 week showed a statistically significant reduction in anxiety-like behaviors, as measured by open field and elevated plus-maze tests. Western blot analysis revealed that CFA-induced upregulation of the levels of pro-inflammatory cytokines interleukin (IL)-1β and tumor necrosis factor α (TNF-α), which played crucial roles in regulating anxiety, returned to normal in the anterior cingulate cortex (ACC) after solanesol treatment. The level of T cell-restricted intracellular antigen-1 (TIA1), a key component of stress granules, also decreased in the ACC. Moreover, immunofluorescence results indicated that solanesol suppressed CFA-induced microglial and astrocytic activation in the ACC. CFA was injected in the hind paws of TIA1 conditional knockout (cKO) mice to confirm whether TIA1 is a potential modulatory molecule that influences pro-inflammatory cytokines and anxiety-like behaviors. Anxiety-like behaviors could not be observed in cKO mice after CFA injection with IL-1β and TNF-α levels not remarkedly increasing. Our findings suggest that solanesol inhibits neuro-inflammation by decreasing the TIA1 level to reduce IL-1β and TNF-α expression, meanwhile inhibiting microglial and astrocytic activation in the ACC and ultimately ameliorating anxiety-like behaviors in mice.

摘要

焦虑症是一种与神经炎症相关的普遍疾病。茄尼醇由于具有抗炎、抗肿瘤和抗溃疡的特性,已显示出积极的效果。本研究旨在确定茄尼醇是否可以改善神经炎症小鼠模型中的焦虑样行为,并确定其作用靶点。用完全弗氏佐剂(CFA)腹腔注射茄尼醇(50mg/kg)1 周的小鼠,通过旷场和高架十字迷宫试验,焦虑样行为明显减少。Western blot 分析显示,CFA 诱导的前扣带回皮质(ACC)中促炎细胞因子白细胞介素(IL)-1β和肿瘤坏死因子α(TNF-α)水平升高,这些细胞因子在调节焦虑中起着关键作用,在用茄尼醇治疗后恢复正常。T 细胞受限内抗原-1(TIA1)的水平也降低,TIA1 是应激颗粒的关键组成部分。此外,免疫荧光结果表明,茄尼醇抑制了 CFA 诱导的 ACC 中的小胶质细胞和星形胶质细胞激活。在 TIA1 条件性敲除(cKO)小鼠的后爪中注射 CFA,以确认 TIA1 是否是影响促炎细胞因子和焦虑样行为的潜在调节分子。在 CFA 注射后,cKO 小鼠中没有观察到焦虑样行为,且 IL-1β和 TNF-α水平没有明显增加。我们的研究结果表明,茄尼醇通过降低 TIA1 水平来抑制神经炎症,从而减少 IL-1β和 TNF-α的表达,同时抑制 ACC 中的小胶质细胞和星形胶质细胞激活,最终改善小鼠的焦虑样行为。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb7c/11432238/7068e933e6f2/ijms-25-10165-g001.jpg

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